A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6536301



Internal ID20909650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:98737831..98740035hg38UCSC Ensembl
chr2:99354294..99356498hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg382205
hg192205
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261683
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6536301
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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